HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946Generated: October 26, 2026
Triethylamine → Methanesulfonic Acid
https://huagongshe.com/reaction/1946
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-[Bis(5-cyclohexyl-4-hydroxy-2-methylphenyl)methyl]benzene-1,2-diol | HCID 15789229 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methanesulfonic Acid | HCID 6395 | — |
| Product | 4-[Bis(5-cyclohexyl-4-hydroxy-2-methylphenyl)methyl]benzene-1,2-diol | HCID 15789229 | — |
Reaction Steps
Bis(5 -cyclohexyl-4-hydroxy-2-methylphenyl)-3,4-dihydroxyphenylmethane(1.0 mole), naphthoquinone-1,2-diazido-5-sulfonyl chloride (2.0 moles) and methanesulfonyl chloride(0.5 moles) were dissolved in dioxane (4,000 g). To the resulting solution, dioxane (1,500 g) having triethylamine (500 g) dissolved therein was added dropwise over 40 minutes at a controlled temperature not higher than 35° C. The precipitating salt was separated by filtration and the thus recovered reaction product was washed and dried to yield a mixed ester of bis(5-cyclohexyl-4-hydroxy-2-methylphenyl)-3,4-dihydroxyphenylmethane with naphthoquinone-1,2-diazido-5-sulfonic acid and methanesulfonic acid; the average degree of esterification was 50% for the quinonediazidosulfonate ester and 12% for the methanesulfonate ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05728504 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-1a28675e5d044056be5059476c8f3ce9 |
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| Source note | uspto-grants-1998_03 |
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